About this role
About the Role Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with Oncology experience who has managed full-service clinical trials within a CRO setting to join our global team. In this role you will provide full-service oversight for clinical projects across global/regional (Ph I-IV) Oncology trials, ensuring delivery on timelines, scope, cost, and quality, and overseeing all functional departments.
You will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team, and will have opportunities to lead international trials as needed. What You'll Do
- Independently lead clinical projects in accordance with the study budget and scope of work; ensure contracted objectives and financial goals are met.
- Serve as the primary client liaison, participating in proposal activities and client presentations; manage the client relationship and project team throughout.
- Involve in proposal strategy, development, costing, and bid defence; oversight of scope, timelines, and budgets.
- Liaise with Project Team and senior management of both Precision and sponsors, including C-level stakeholders, to drive quality and ensure coordinated execution.
- Handle and lead all aspects of a clinical research trial or trials; total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics.
- Prepare project status updates for clients and management; identify key deliverables and performance metrics and escalate as needed.
- Be an active member of the Project Team with the goal to contribute towards efficient management and execution of trials.
- Prepare and review protocols and other study documentation such as project plans, informed consents, site contracts and budgets.
- You may be called upon to run international trials; travel domestically and internationally as required. What We're Looking For
- Degree or similar life science qualification, or equivalent combination of education and experience.
- Previous experience in a full-service/global Project Management role in the CRO industry is essential.
- Extensive experience in Clinical Operations in a CRO, and at least 4 years full-service Project Management experience in a clinical trial setting.
- Experience managing studies within Oncology.
- Working understanding of GCP/ICH guidelines and the clinical development process.
- Ability to travel domestically and internationally including overnight stays.
- Proficient in English (written and spoken).
- Strong presentation skills.
- Proficient computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).
- Proven ability to develop positive working relationships with individuals and teams internally and externally.
- Demonstrated core understanding of medical terminology and clinical trial activities as it relates to execution of a clinical development plan.